• Stat Summaries. Mastery provides a passive bonus to your character based on your specialization. Mastery: Chaotic Energies causes your spells to deal an additional amount of random damage and also reduces the damage you take by a random amount. Haste increases attack and spell casting speed, adds additional damage and healing to DoTs and HoTs, and reduces the GCD.
  • XPOff is the result of a merge with our old home, Twinkinfo. The goal of the website is to function as the primary hub for our community, and it is currently a safe harbor for those of us interested in the ancient, but still very much alive art of twinking in World of Warcraft.
  • Oct 11, 2019 It is not a secret, that current warlock design is bad across the board. The reason why warlock suffers in BFA lies not only in bad damage dealing mechanics(All melee players, please take a note that damage dealing mechanics is not the same as bad damage numbers). Like i said before warlocks suffer from bad damage dealing mechanics. To future adress this issue let’s just take a look at.
  • Apr 18, 2017  Welcome to /r/wow, a subreddit about the video game World of Warcraft! Class with the highest DMG number? (Not DPS) submitted 2 years ago by FreddyRamson. If not ele then I'd probably go with fire mage. If you go with shaman, then lava burst is something you'll almost always be casting so those crits will be constant.
  • Latest World of Warcraft AddOns for Patch 8.3 WowMatrix saves you hours of time. Before opening World of Warcraft, just fire up WowMatrix and let it update your WoW AddOns quickly and safely. Here are just some of the many WoW AddOns supported by WowMatrix, with more being added daily.
IUPAC name
Other names
  • 1118-68-9
  • 653
ECHA InfoCard100.012.971
EC Number
  • 214-267-8
  • C01026
RTECS number
CompTox Dashboard(EPA)
  • InChI=1S/C4H9NO2/c1-5(2)3-4(6)7/h3H2,1-2H3,(H,6,7)
  • CN(C)CC(O)=O
Molar mass103.121 g·mol−1
AppearanceWhite crystals
Density1.069 g/mL
Melting point 178 to 182 °C (352 to 360 °F; 451 to 455 K)
Boiling point 175.2 °C (347.4 °F; 448.3 K)
GHS pictograms
GHS Signal wordWarning
Lethal dose or concentration (LD, LC):
>650 mg kg−1(oral, rat)
Related compounds
Related alkanoic acids
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
verify (what is ?)
Infobox references

I have 'combat text' enabled in the interface, I've gone through and disabled all of my add-on's, still nothing. I deleted my cache file (figured why not?) and relogged multiple times. Still, nothing. Damage numbers appear on me (IE: -388) when I'm hit, healing numbers appear on me, but there's no numbers when I attack anything. Any help or tips? Tank, Healer, Damage Bare-knuckle brawlers whose no-weapon styles were born in ancient Pandaria, monks are as diverse as the energy that surrounds them. They can shoulder deadly attacks through the haze of their brews, heal broken chi flows, and beat their enemies with wind-quick fists and feet.

Dimethylglycine (DMG) is a derivative of the amino acidglycine with the structural formula (CH3)2NCH2COOH. It can be found in beans and liver. It can be formed from trimethylglycine upon the loss of one of its methyl groups. It is also a byproduct of the metabolism of choline.

When DMG was first discovered, it was referred to as Vitamin B16, but, unlike true B vitamins, deficiency of DMG in the diet does not lead to any ill-effects and it is synthesized by the human body in the citric acid (or Krebs) cycle meaning it does not meet the definition of a vitamin.


Dimethylglycine has been suggested for use as an athletic performance enhancer, immunostimulant, and a treatment for autism, epilepsy, or mitochondrial disease.[2] There is no evidence that dimethylglycine is effective for treating mitochondrial disease.[3] Published studies on the subject have shown little to no difference between DMG treatment and placebo in autism spectrum disorders.[4][5]

Biological activity[edit]

Dimethylglycine has been found to act as an agonist of the glycine site of the NMDA receptor.[6]



This compound is commercially available as the free form amino acid, and as the hydrochloride salt [2491-06-7 ]. DMG may be prepared by the alkylation of glycine via the Eschweiler–Clarke reaction. In this reaction, glycine is treated with aqueous formaldehyde in formic acid that serves as both solvent and reductant. Hydrochloric acid is added thereafter to give the hydrochloride salt. The free amino acid may have been obtained by neutralization of the acid salt, which has been performed with silver oxide.[7]

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H2NCH2COOH + 2 CH2O + 2 HCOOH → (CH3)2NCH2COOH + 2 CO2 + 2 H2O


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  1. ^'dimethylglycine - Compound Summary'. PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification. Retrieved 24 April 2012.
  2. ^'Dimethylglycine'. About Herbs, Botanicals & Other Products. Memorial Sloan–Kettering Cancer Center. December 8, 2009.
  3. ^Pfeffer, Gerald; Majamaa, Kari; Turnbull, Douglass M.; Thorburn, David; Chinnery, Patrick F. (2012-04-18). 'Treatment for mitochondrial disorders'. The Cochrane Database of Systematic Reviews (4): CD004426. doi:10.1002/14651858.CD004426.pub3. ISSN1469-493X. PMID22513923.
  4. ^Bolman WM, Richmond JA (June 1999). 'A double-blind, placebo-controlled, crossover pilot trial of low-dose dimethylglycine in patients with autistic disorder'. Journal of Autism and Developmental Disorders. 29 (3): 191–4. doi:10.1023/A:1023023820671. PMID10425581.
  5. ^Kern JK, Miller VS, Cauller PL, Kendall PR, Mehta PJ, Dodd M (March 2001). 'Effectiveness of N,N-dimethylglycine in autism and pervasive developmental disorder'. Journal of Child Neurology. 16 (3): 169–73. doi:10.1177/088307380101600303. PMID11305684.
  6. ^Lin, Jen-Cheng; Chan, Ming-Huan; Lee, Mei-Yi; Chen, Yi-Chyan; Chen, Hwei-Hsien (2016). 'N,N-dimethylglycine differentially modulates psychotomimetic and antidepressant-like effects of ketamine in mice'. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 71: 7–13. doi:10.1016/j.pnpbp.2016.06.002. ISSN0278-5846. PMID27296677.
  7. ^Clarke, H. T.; Gillespie, H. B.; Weisshaus, S. Z. (1933). 'The Action of Formaldehyde on Amines and Amino Acids'. Journal of the American Chemical Society. 55 (11): 4571. doi:10.1021/ja01338a041.

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